ライフサイエンスコーパス: glucosidase

1 hibiting also butyrylcholinesterase and beta-glucosidase.

2 g predicted a high affinity of CGA for alpha-glucosidase.

3 chanism-based covalent inhibitor of an alpha-glucosidase.

4 .2 nM) of the Thermotoga maritima TmGH1 beta-glucosidase.

5 coincubated with the recombinant human alpha-glucosidase.

6 l) displayed strong inhibition towards alpha-glucosidase.

7 e aglycones produced by hydrolysis with beta-glucosidase.

8 potent inhibitors of alpha-amylase and alpha-glucosidase.

9 tural inhibitors for alpha-amylase and alpha-glucosidase.

10 obioside as the strongest inhibitor of alpha-glucosidase.

11 od covalent inhibitors of a GH13 yeast alpha-glucosidase.

12 luble beta-glucosidase and GPI-anchored beta-glucosidase.

13 ding endoglucanases, exoglucanases, and beta-glucosidases.

14 interpret the glucose dependence of GH1 beta-glucosidases.

15 the beetle myrosinase from other insect beta-glucosidases.

16 up to 76% sequence similarity to other beta-glucosidases.

17 for other glycoside hydrolase family 3 beta-glucosidases.

18 tly modify the nucleophile of retaining beta-glucosidases.

19 understand the glucose tolerance in GH3 beta-glucosidases.

20 he C-ring was related to inhibition of alpha-glucosidases.

21 so has soluble and membrane-bound xyloglucan glucosidases.

22 dase (3.42), beta-xylosidase (0.07) and beta-glucosidase (0.28) on low-cost copra meal (CM) in SSF.

23 n-degrading extracellular enzymes (beta-1, 4-glucosidase, 1, 4-beta-cellobiosidase, beta-D-xylosidase

24 Furthermore, only one beta-glucosidase 12 homolog has been characterized so far.

25 n of a sulfur deficiency-activated gene beta-glucosidase 28 (BGLU28).

26 Anthocyanin-rich extracts inhibited alpha-glucosidase (37.8%), alpha-amylase (35.6%), dipeptidyl p

27 ng of pancreatic lipase (74.5%) and of alpha-glucosidase (98.2%).

28 Here, the extremophilic beta-glucosidase A from Halothermothix orenii, (BglA) has bee

29 While BGLC1 (At5g20950; for beta-glucosidase active against xyloglucan 1) is responsible

30 ect in inhibiting i) alpha-amylase and alpha-glucosidase activities and ii) colorectal cancer cell li

31 lactate dehydrogenase and lysosomal alpha-d-glucosidase activities was also tested.

32 nhibitory effects on alpha-amylase and alpha-glucosidase activities.

33 aluating the lipase, alpha-amylase and alpha-glucosidase activities.

34 erived OC supported elevated phosphatase and glucosidase activities.

35 -) mice, pharmacological inhibition of alpha-glucosidase activity almost completely abolished residua

36 esponse functions were investigated for beta-glucosidase activity and isoflavone contents.

37 noterpenes inhibited alpha-amylase and alpha-glucosidase activity and stimulated glucose uptake and l

38 al DeltaSPD0247 strain had reduced 6-phospho-glucosidase activity and was attenuated in growth on cel

39 A. oryzae IOC 3999/1998 expressed beta-glucosidase activity at 10.7 times higher than M. purpur

40 he inhibition of the alpha-amylase and alpha-glucosidase activity facilitates the maintenance of circ

41 The beta-Glucosidase activity has been constant over time, showin

42 g Gaucher disease and the regulation of beta-glucosidase activity in general.

43 nd 17 muM, and also inhibited lysosomal beta-glucosidase activity in live cells at low-micromolar con

44 resulting in deficient lysosomal acid-alpha-glucosidase activity in patients, and a progressive decl

45 Extracts with IC50 for alpha-glucosidase activity in the 0.010-0.079mgmL(-1) range sh

46 We then used HPLC-MS/MS to assess the beta-glucosidase activity of purified enzymes on p-nitropheny

47 The beta-Glucosidase activity was 6 and 14% higher with manure th

48 beta-Glucosidase activity was measured using the synthetic su

49 ential inhibition of alpha-amylase and alpha-glucosidase activity was observed in response to polarit

50 The beta-glucosidase activity was reduced through soybean slurry

51 Ectomycorrhizal fungal richness and beta-glucosidase activity were strongly reduced by burning an

52 and the potential ability to modulate alpha-glucosidase activity were tested.

53 CWEN, and enzyme activities especially beta-Glucosidase activity were the key determinants of MCC.

54 he strongest inhibitory effect against alpha-glucosidase activity with IC(50) 0.08 +/- 0.002 mg/mL.

55 glucosidase enzymes (Delta3betaG) lacks beta-glucosidase activity, but efficiently induces cellulase

56 We show that alpha-glucosidase activity, i.e. glycogen debranching and/or l

57 he active site completely abolishes the beta-glucosidase activity.

58 lycosidase activity (GA) by 13.0%, alpha-1,4-glucosidase (AG) by 19.6%, beta-1,4-glucosidase (BG) by

59 vities of the three lysosomal enzymes (alpha-glucosidase (AG), beta-galactosidase (B-GAL) and beta-N-

60 Four glycosidases, alpha-glucosidase (AG), beta-glucosidase (BG), beta-xylosidase

61 dehydrogenase (DHA) and extracellular alpha-glucosidase (alpha-Glu) and protease (PRO) enzymes were

62 toprostanes (PhytoPs) on four enzymes: alpha-glucosidase, alpha-amylase, acetylcholinesterase, and bu

63 The inhibition of alpha-glucosidase, alpha-amylase, and angiotensin-converting I

64 The inhibition of alpha-glucosidase, alpha-amylase, lipase, cyclooxygenases-1 an

65 To promote their release, beta-glucosidase, alpha-arabinosidase, and alpha-rhamnosidase

66 ted with metabolic syndrome, including alpha-glucosidase, amylase and lipase and exhibited antioxidan

67 <= 0.05) in peel and pulp tissues (85% alpha-glucosidase and 8% alpha-amylase inhibition).

68 rpm), significantly (p < 0.05) higher alpha-glucosidase and acetylcholinesterase inhibition activiti

69 dant activities for free fraction, and alpha-glucosidase and acetylcholinesterase inhibition for whol

70 scavenging activity and alpha-amylase, alpha-glucosidase and aldose reductase inhibitory activity wer

71 nols from guarana were able to inhibit alpha-glucosidase and alpha-amylase activities.

72 For this purpose, alpha-glucosidase and alpha-amylase assays were assessed; amon

73 ted glucoses were studied as potential alpha-glucosidase and alpha-amylase inhibitors.

74 th evaluation of in vitro antioxidant, alpha-glucosidase and alpha-amylase inhibitory activities of v

75 rdolino extracts exhibited the highest alpha-glucosidase and alpha-amylase inhibitory activity with I

76 h can be counteracted by inhibition of alpha-glucosidase and alpha-amylase, both involved in the carb

77 antioxidant activities, inhibition of alpha-glucosidase and alpha-amylase, inhibition of angiotensin

78 as selective competitive inhibitors of beta-glucosidase and are promising candidates as pharmacologi

79 al design to optimise the production of beta-glucosidase and convert glycosidic isoflavones in aglyco

80 green olives is due to the activity of beta-glucosidase and esterase during the first months of stor

81 alactosidase, alpha-fucosidase, soluble beta-glucosidase and GPI-anchored beta-glucosidase.

82 capacity in inhibiting alpha-amylase, alpha-glucosidase and HT29 cell growth.

83 e and comparable and lower activity on alpha-glucosidase and hyaluronidase, respectively.

84 The free beta-glucosidase and immobilised cells containing the enzyme

85 e highest inhibition of alpha-amylase, alpha-glucosidase and lipase (IC50: 0.38mg/mL, 0.87mug/mL and

86 L-cholesterol peroxidation, as well as alpha-glucosidase and lipase activities were demonstrated, the

87 as well as evaluation of inhibition of alpha-glucosidase and lipase activities.

88 ome-associated enzymes (alpha-amylase, alpha-glucosidase and lipase) was evaluated.

89 pinnatifida has a potential to inhibit alpha-glucosidase and may be used as a bioactive food ingredie

90 tory activities towards alpha-amylase, alpha-glucosidase and tyrosinase.

91 s inhibited the enzymes alpha-amylase, alpha-glucosidase and xanthine oxidase.

92 1 genes co-localize with genes encoding beta-glucosidases and ATP-binding cassette transporters, high

93 ) crystal structures, we determine that most glucosidases and beta-mannosidases preferentially bind t

94 lactosidase, soluble and membrane-bound beta-glucosidases and two alpha-fucosidases.

95 study was to monitor olive hydrolytic (beta-glucosidase) and oxidative (peroxydase, POX, and polyphe

96 in glucocerebrosidase (GBA, a retaining beta-glucosidase), and deficiency in GBA constitutes the larg

97 nzyme, enzyme type (cellulase, pectinase, ss-glucosidase), and hydrolysis time (1, 4, 8, 24 h) on the

98 t activity, and greater alpha-amylase, alpha-glucosidase, and ACE inhibitory activity than the pasteu

99 inhibitory potential of alpha-amylase, alpha-glucosidase, and dipeptidyl peptidase III (DPP III) enzy

100 ritol B epoxide is an inhibitor of acid beta-glucosidase, and lowers glucosylceramide degradation.

101 argets, including islet amyloid polypeptide, glucosidases, and cholinesterases.

102 stinct for antioxidant activity, ACE-, alpha-glucosidase-, and Kunitz trypsin-inhibitory activity.

103 beta-Glucosidases are enzymes that hydrolyze beta-glycosidic

104 However, most beta-glucosidases are feedback inhibited by the glucose produ

105 beta-Glucosidases are known to play a role in abiotic stresse

106 tivity profiles on disaccharides, these beta-glucosidases are not functionally equivalent.

107 ribes novel preparations of immobilized beta-glucosidase as highly stable and active catalysts for in

108 y-2-fluoro-beta-glucosides react with a beta-glucosidase at rates differing by 10(6)-fold, despite th

109 Additionally, the beta-glucosidase BABG that is present in Brassica rapa but ab

110 In addition, soluble beta-glucosidase BdBGLC1 (Bd1g08550) complemented a glucosida

111 ur) are both produced by E. coli, while beta-glucosidase (beta-gluco) is produced by Enterococcus spp

112 aucher disease is caused by mutations in the glucosidase, beta, acid gene that encodes glucocerebrosi

113 Glucosidase, beta, acid mutations often cause protein mi

114 ll wall metabolism (beta-galactosidase, beta-glucosidase, beta-amylase, chitinase, pectate lyase (PL)

115 or irreversible inhibition of retaining beta-glucosidases, beta-aziridine ABPs do not.

116 The enzyme is a beta-glucosidase/beta-xylosidase that also shows beta-galacto

117 lpha-1,4-glucosidase (AG) by 19.6%, beta-1,4-glucosidase (BG) by 11.1%, beta-1,4-xylosidase (BX) by 2

118 r glycosidases, alpha-glucosidase (AG), beta-glucosidase (BG), beta-xylosidase (BX), cellobiohydrolas

119 potential activities of cellulase (CL), beta-glucosidase (BG), lignin peroxidase (LiP), and manganese

120 ize a family 3 glycosyl hydrolase (GH3) beta-glucosidase (Bgl) produced by Malbranchea pulchella (MpB

121 his study, we characterized a 6-phospho-beta-glucosidase (BglA3) encoded by SPD_0247.

122 be in an operon with a putative phospho-beta-glucosidase (bglB) downstream and a predicted antitermin

123 High-resolution alpha-glucosidase biochromatograms of these extracts allowed f

124 primarily of stereochemistry-retaining beta-glucosidases but also contains a subfamily of beta-N-ace

125 tural basis of glucose tolerance in GH1 beta-glucosidases but also demonstrate a strategy to improve

126 opsis thaliana contain large amounts of beta-glucosidases, but the physiological functions of ER bodi

127 fy both catalytic residues of retaining beta-glucosidases by the combined use of cyclophellitol beta-

128 zymes of intact heterotrophic biofilms, beta-glucosidase (carbon-cycling) and l-leucin aminopeptidase

129 beta-glucosidases catalyze the hydrolysis beta-1,4, beta-1,3

130 to non-homologous (putative) retaining beta-glucosidases categorized in GH1 and GH116: GBA2, GBA3, a

131 terized the corresponding GH1 6-phospho-beta-glucosidase, Cel1A.

132 on of both enzymes, as a membrane-bound beta-glucosidase could specifically digest soluble xyloglucan

133 D) is a metabolic myopathy due to acid alpha-glucosidase deficiency and characterized by extensive gl

134 A is, thus, preferable as an industrial beta-glucosidase despite its lower activity caused by transgl

135 iated uptake of recombinant human acid-alpha-glucosidase during ERT in mice with Pompe disease follow

136 beta-Glucosidases enhance enzymatic biomass conversion by rel

137 the beta-glucoside permease (bglP) and beta-glucosidase enzyme (bglB) in 5448, we showed that bglB,

138 ntrations were associated with enhanced beta-glucosidase enzyme activities (V max ) but short-term dr

139 showed more than 80% inhibition of the alpha-glucosidase enzyme at a concentration of 40mg/mL (dry sa

140 matic activities, results show that the beta-glucosidase enzyme is the key enzyme responsible for the

141 se compounds, which are bioactivated by beta-glucosidase enzymes (BGDs).

142 assa mutant carrying deletions of three beta-glucosidase enzymes (Delta3betaG) lacks beta-glucosidase

143 mutant lacking genes encoding both the beta-glucosidase enzymes and cellodextrin transporters (Delta

144 -4B is an iminosugar that inhibits the alpha-glucosidase family of enzymes and subsequently the foldi

145 The highest production of beta-glucosidase for both strains occurred when adding 10 mL

146 Finally, Bgl3D is the crucial beta-glucosidase for XyG utilization.

147 me and the immobilised cells containing beta-glucosidase, for 2h at 40 degrees C, promoted efficient

148 most potent (IC50: 0.25mug/mL) against alpha-glucosidase; Fraction IV from black turtle bean was the

149 re assayed to catalyze the process, and beta-glucosidase from Aspergillus niger was selected.

150 to be low micromolar inhibitors of the alpha-glucosidase from baker's yeast with Ki's near to 2 muM.

151 ctional characterization of CsBGlu12, a beta-glucosidase from Crocus sativus.

152 An intracellular beta-glucosidase from Debaryomyceshansenii UFV-1 was produced

153 expressed OeGLU, an oleuropein-specific beta-glucosidase from olive (Olea europaea), had enzymatic ki

154 i-casuarine is a strong inhibitor of alpha-d-glucosidase from rice and of rat intestinal sucrase.

155 rent Arabidopsis (Arabidopsis thaliana) beta-glucosidases from glycoside hydrolase family 3.

156 y of the industrially relevant family 3 beta-glucosidases from Hypocrea jecorina, HjCel3A and HjCel3B

157 somal glycogen-hydrolyzing enzyme acid alpha-glucosidase (GAA) activity, which results in lysosomal g

158 arily the liver and kidney, while acid alpha-glucosidase (GAA) deficiency in GSD II causes primarily

159 or gene replacement therapy with acid alpha-glucosidase (GAA) has achieved only partial efficacy in

160 d to and degraded in lysosomes by acid alpha-glucosidase (GAA) in mammals, but it is unclear why and

161 disorder characterized by lack of acid-alpha glucosidase (GAA) resulting in ubiquitous lysosomal glyc

162 caused by mutations in lysosomal acid alpha-glucosidase (Gaa), manifests rapidly progressive fatal c

163 uscles of young-, mid-, and late-stage alpha-glucosidase (GAA)-deficient mice.

164 ether with a bifunctional 6-phospho-beta-gal/glucosidase, Gan1D.

165 dated the method by using the retaining beta-glucosidase GBA (CAZy glycosylhydrolase family GH30) and

166 The lysosomal acid beta-glucosidase GBA1 and the non-lysosomal beta-glucosidase

167 -glucosidase GBA1 and the non-lysosomal beta-glucosidase GBA2 degrade glucosylceramide (GlcCer) to gl

168 xide (CBE), as well as the nonlysosomal beta-glucosidase (GBA2) inhibitor N-butyldeoxygalactonojirimy

169 dase (GBA), and the cytosolic retaining beta-glucosidase, GBA3.

170 caused by insufficient activity of acid beta-glucosidase (GCase) and the resultant glucosylceramide (

171 Defective lysosomal acid beta-glucosidase (GCase) in Gaucher disease causes accumulati

172 CBE-N2a) was created by inhibiting acid beta-glucosidase (GCase) in N2a cells with conduritol B epoxi

173 eading to functional deficiency of acid-beta-glucosidase (GCase).

174 that encodes the lysosomal enzyme acid beta-glucosidase (GCase).

175 used by mutations in GBA1 encoding acid beta-glucosidase (GCase).

176 erococcus faecalis, encodes a 6-phospho-beta-glucosidase (GenA) and a phosphotransferase system perme

177 The acid beta-glucosidase (glucocerbrosidase (GCase)) binding sequence

178 OH led to an increase of 10% in both alpha-glucosidase (>99%) and alpha-amylase (>=70%).

179 confirmed their high affinity towards alpha-glucosidase, highlighting a static quenching mechanism.

180 oved the functional properties of a GH1 beta-glucosidase highly expressed by Trichoderma harzianum (T

181 lings with a rare genetic defect in ER alpha-glucosidase I (ER Glu I) who showed resistance to viral

182 lacking Erv41-Erv46 function, the ER enzyme glucosidase I (Gls1) was mislocalized and degraded in th

183 ic that inhibits endoplasmic reticulum alpha-glucosidase I and II enzymes resulting in improper glyco

184 -glycosylation trimming pathway involving ER glucosidases I and II.

185 was particularly active against yeast alpha-glucosidase (IC(50) = 1.53 mug/mL), acting through a non

186 on (alpha-amylase: IC(50)-42.34 ug/mL; alpha-glucosidase: IC(50):63.89 ug/mL), basal uptake of glucos

187 pea showed inhibitory activity against alpha-glucosidase (IC50 6967 +/- 343 and 2885 +/- 85.4 mug/ml,

188 (bran) and 148.23 mug/ml (hulls)] and alpha-glucosidase [IC50, 62.1 mug/ml (bran) and 68.14 mug/ml (

189 Screening a library of over 100 beta-glucosidases identified a number of enzymes that catalyz

190 structures of the main ERQC enzyme, ER alpha-glucosidase II (alpha-GluII; from mouse), alone and in c

191 and genetic approaches, we demonstrate that glucosidase II (GII) mediates glycan trimming of TRPP2.

192 The non-catalytic beta subunit of glucosidase II (GIIbeta) is encoded by PRKCSH, one of th

193 sylation of N-glycans, and oppositely acting glucosidase II (GlucII), and that vIL-6 can promote prot

194 ycoprotein glucosyltransferase 1 (UGGT1) and glucosidase II (GlucII).

195 with a missense mutation in GANAB, encoding glucosidase II subunit alpha (GIIalpha).

196 unctions as the noncatalytic beta subunit of Glucosidase II, an endoplasmic reticulum (ER)-resident e

197 e we show that PYK10, the most abundant beta-glucosidase in A. thaliana root ER bodies, hydrolyzes in

198 ell as a decrease in the inhibition of alpha-glucosidase in both extracts, when compared to undigeste

199 edly enhanced expression of human acid-alpha-glucosidase in nonhuman primates.

200 The most abundant beta-glucosidase in the mesophilic fungus Hypocrea jecorina i

201 Interestingly, expression of individual beta-glucosidases in Escherichia coli K-12 enabled this non-c

202 in tannins (16C) induced a more potent alpha-glucosidase inhibition (pIC(50) = 5.3 +/- 0.1).

203 garding the in vitro alpha-amylase and alpha-glucosidase inhibition activities of extracts derived fr

204 ters that affect the alpha-amylase and alpha-glucosidase inhibition activities of the extracts.

205 e been shown to have alpha-amylase and alpha-glucosidase inhibition activities.

206 alpha-Glucosidase inhibition activity, cell viability and ther

207 l scavenging, beta-carotene bleaching, alpha-glucosidase inhibition and greatest amount of TPC.

208 ing, beta-carotene bleaching activity, alpha-glucosidase inhibition and the highest total phenolic co

209 one extracts of seaweeds were used for alpha-glucosidase inhibition assay hyphenated with high perfor

210 variate data analysis, high-resolution alpha-glucosidase inhibition assays and HPLC-HRMS-SPE-NMR with

211 The alpha-glucosidase inhibition in FL was higher than that of FQ

212 docking was carried out to investigate alpha-glucosidase inhibition mechanisms.

213 ore investigated using high-resolution alpha-glucosidase inhibition profiling combined with high-perf

214 ) activity, however, a 10% increase in alpha-glucosidase inhibition was observed in irradiated (2.5 k

215 30-50% alpha-glucosidase inhibition was observed in ultrasound, Flavo

216 ved on antidiabetic (alpha-amylase and alpha-glucosidase inhibition) activity, however, a 10% increas

217 tyrylcholinesterase, tyrosinase, amylase and glucosidase inhibition) were used for screening of peppe

218 anticancer activity, alpha-amylase and alpha-glucosidase inhibition, angiotensin-converting-enzyme (A

219 stigated, as well as alpha-amylase and alpha-glucosidase inhibition, antihypertensive, antioxidant an

220 lified roasting-induced differences in alpha-glucosidase inhibition, CGA showed a decreasing trend up

221 were in vitro digested and tested for alpha-glucosidase inhibition, to explore their antidiabetic po

222 so showed a high (~ 98%) potential for alpha-glucosidase inhibition.

223 ter fraction (WF) of ME was a stronger alpha-glucosidase inhibitor (EC50 2.9 mug/mL) than quercetin,

224 SMD, 0.33 [95% CI, 0.13 to 0.52]), and alpha-glucosidase inhibitor (SMD, 0.35 [95% CI, 0.12 to 0.58])

225 The effect of the alpha-glucosidase inhibitor acarbose on cardiovascular outcome

226 l" analogue would be a potent retaining beta-glucosidase inhibitor for those enzymes reacting through

227 tive synthesis of nectrisine, a potent alpha-glucosidase inhibitor, was carried out starting from but

228 WF was a competitive alpha-glucosidase inhibitor.

229 increased amount of quercetin, a known alpha-glucosidase inhibitor.

230 Iminosugars, which are glucosidase inhibitors, can interfere with the initial s

231 rily by adding or adjusting metformin, alpha-glucosidase inhibitors, thiazolidinediones, or insulin,

232 litol aziridine-both covalent retaining beta-glucosidase inhibitors-we postulated that the correspond

233 es revealed to be potent and selective alpha-glucosidase inhibitors.

234 The alpha-glucosidase inhibitory activities of the VJ and FVJ were

235 lues following fermentation, while the alpha-glucosidase inhibitory activities ranged from 95.2 to 19

236 X2C gave a subfraction, with enhanced alpha-glucosidase inhibitory activity (IC50=6.15mug/mL), with

237 -bioassay/HPLC-HRMS-SPE-NMR showed the alpha-glucosidase inhibitory activity of A. nodosum, F. vesocu

238 The antioxidant capacity and the alpha-glucosidase inhibitory activity of the duodenal extract

239 oside-A showed concentration-dependent alpha-glucosidase inhibitory activity with IC50=35.01 mug/ml.

240 identification of three analytes with alpha-glucosidase inhibitory activity, and subsequent HPLC-HRM

241 Samples showing more than 60% alpha-glucosidase inhibitory activity, at a concentration of 1

242 H), polyphenol content (GAE) and yeast alpha-glucosidase inhibitory activity.

243 ere screened for their antioxidant and alpha-glucosidase inhibitory activity.

244 velopment of new functional foods with alpha-glucosidase inhibitory activity.

245 ibly due to the presence of intestinal alpha-glucosidase inhibitory and augmenting cellular glucose u

246 Addition of 8U of beta-glucosidase into soymilk significantly increased the con

247 A range of enzymes, namely beta-glucosidase, invertase, beta-galactosidase, and catalase

248 beta-Glucosidase is an ubiquitous enzyme which has enormous b

249 In the present work Aspergillus niger beta-glucosidase is immobilized within nanoscale polymeric ma

250 s found that only one of four predicted beta-glucosidases is required in a physiological context.

251 abetes framework, the extract inhibits alpha-glucosidase (K(i) = 166.9 ug/mL) and aldose reductase (K

252 rological legacy alters the response of beta-glucosidase kinetics (i.e. type of inhibition) to short-

253 l-NBDNJ is able to enhance lysosomal alpha-glucosidase levels in Pompe disease fibroblasts, either

254 lic syndrome, including alpha-amylase, alpha-glucosidase, lipase and hydroxyl methyl glutaryl CoA red

255 compounds did not affect inhibition of alpha-glucosidase (maltase) activity, which remained relativel

256 In vitro digested coffee inhibited alpha-glucosidase more effectively, compared to undigested sam

257 ucosidase BdBGLC1 (Bd1g08550) complemented a glucosidase mutant.

258 and biallelic MOGS (mannosyl-oligosaccharide glucosidase) mutations (GenBank: NM_006302.2; c.[65C>A;

259 Remarkably, some beta-glucosidases of the glycoside hydrolase (GH) 1 family ar

260 screen, and the Exg1 gene (coding for a beta-glucosidase) of D. bruxellensis was cloned and purified.

261 ct and its inhibiting activity against alpha-glucosidase, pancreatic lipase and hyaluronidase were de

262 enzymatic in vitro inhibition tests of alpha-glucosidase, pancreatic lipase, acetylcholinesterase and

263 ), anti-diabetic (anti-alpha-amylase, -alpha-glucosidase, -pancreatic lipase) and antioxidant potenti

264 e insect but can be cleaved by a spruce beta-glucosidase, PgbetaGLU-1, which releases the active agly

265 surfaces with OM inputs had the highest beta-glucosidase, phosphatase, NAGase and cellobiohydrolase a

266 yl acetate fraction inhibited in vitro alpha-glucosidase (pIC(50) = 4.8 +/- 0.1), an enzyme involved

267 beta-glucosidases play a critical role among the enzymes in e

268 The ability of olive endogenous enzymes beta-glucosidase, polyphenol oxidase (PPO) and peroxidase (PO

269 These differences could be due to beta-glucosidase, POX and PPO activities changes during olive

270 kdown of beta-1, 4-glycosidic linkages, beta-glucosidases produce free fermentable glucose and allevi

271 Inhibition of acid beta-glucosidase promoted faster axonal elongation in an in v

272 f the full-length GAA transcript, acid-alpha-glucosidase protein, and enzyme activity in all patients

273 -bound drug for recombinant human alpha acid glucosidase (rhGAA) in plasma from patients suffering fr

274 this benefit, most characterised fungal beta-glucosidases show weak activity at high glucose concentr

275 lpha-amylase, but potent inhibitors of alpha-glucosidase, showing low-micromolar IC(50) values, far l

276 n properties against alpha-amylase and alpha-glucosidases, showing different inhibition constants (K(

277 perior inhibition of alpha-amylase and alpha-glucosidase than foxtail millet cultivars.

278 o-component defense system comprising a beta-glucosidase that activates oleuropein into a toxic gluta

279 ) is an intestinal membrane-associated alpha-glucosidase that breaks down di- and oligosaccharides to

280 ta-glucanase, BT3312, and a periplasmic beta-glucosidase that targets primarily 1,6-beta-glucans.

281 rients involves the action of 6-phospho-beta-glucosidase to convert them into usable monosaccharaides

282 ion of ICHO and ICOOH derivative pools after glucosidase treatment revealed that, in response to AgNO

283 resence of active polyphenoloxidase and beta-glucosidase was determined by HPLC and UV-Visible spectr

284 activity of pectin methyl esterase and beta-glucosidase was enhanced in ET-treated berry skins, sugg

285 of the samples, only the inhibition of alpha-glucosidase was preserved.

286 looxygenase 1 and -2, as well as amylase and glucosidase was recorded for the breads enriched with th

287 Inhibition of alpha-amylase and alpha-glucosidase was the highest at 65 and 85 degrees C, i.e.

288 e dehydrogenase activity, but not of alpha-d-glucosidase, was observed.

289 east cells containing the intracellular beta-glucosidase were immobilised in calcium alginate.

290 y properties against alpha-amylase and alpha-glucosidase were investigated.

291 mutation(s) in GBA, which encodes acid beta-glucosidase, were recruited at the SZMC Gaucher Clinic.

292 osomal acid maltase, two major hepatic alpha-glucosidases, were unaltered in L-G6pc(-/-) mice, pharma

293 rated uncompetitive inhibitors against alpha-glucosidase, while EAEP, AEP, and HEX-AEP (used as contr

294 se tolerance and stimulation of the GH1 beta-glucosidases will be crucial to improve their applicatio

295 lted in the thermo-stabilization of the beta-glucosidase with an increase in optimum temperature and

296 of fucoxanthin significantly inhibited alpha-glucosidase with IC(50) value 0.047 +/- 0.001 mg/mL.

297 Beta-glucosidase with putative algicidal capability was ident

298 mary and tertiary structures of two GH1 beta-glucosidases with distinct glucose dependence, some puta

299 ractions X1C and X2C notably inhibited alpha-glucosidase, with IC50=9.89 and 8.05mug/mL, respectively

300 HjCel3A and other structurally similar beta-glucosidases would have a significant economic effect on